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Inkjet ink comprising gallium naphthalocyanine dye

a gallium naphthalocyanine and inkjet technology, applied in the field of infrared (ir) dyes, can solve the problems of no longer preventing scanning of labels, no prior art dyes can be formulated into ink compositions suitable for netpage or hy, and commercially available and/or prior art inks

Inactive Publication Date: 2007-02-15
BASF AG
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Furthermore, if the tags are compact and massively replicated (“omnitags”), then label damage no longer prevents scanning.
However, none of the prior art dyes can be formulated into ink compositions suitable for use in netpage or Hyperlabel™ systems.
In particular, commercially available and / or prior art inks suffer from one or more of the following problems: absorption at wavelengths unsuitable for detection by near-IR sensors; poor solubility or dispersibility in aqueous solvent systems; or unacceptably high absorption in the visible part of the spectrum.

Method used

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  • Inkjet ink comprising gallium naphthalocyanine dye
  • Inkjet ink comprising gallium naphthalocyanine dye
  • Inkjet ink comprising gallium naphthalocyanine dye

Examples

Experimental program
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Effect test

example 1

[0395] Hydroxygallium naphthalocyaninetetrasulfonic acid 2 and its corresponding triethylammonium salt 3 were prepared according to the procedure outlined in Scheme 1.

a) 1,2-di(naphthalocyaninatogalliumoxo)ethane (NcGaOCH2CH2OGaNc) 1

[0396] A solution of gallium chloride (0.735 g; 4.18 mmol) in anhydrous toluene (5 mL) was cooled in an ice bath and treated with sodium methoxide portionwise with stirring. Ethylene glycol (5 mL) was then added slowly while cooling the reaction mixture. After stirring for 10 min, naphthalene-1,2-dicarbonitrile (2.98 g; 16.7 mmol) was added all at once as a solid and the resulting slurry was heated initially to distil off the toluene and methanol. Following this, the bath temperature was raised to 190-195 ° C. to induce the cyclotetramerisation to take place. The reaction mixture was maintained at this temperature for 2.5 h and then allowed to cool to room temperature. The resulting green / brown slurry was diluted with absolute ethanol (10 mL) and the ...

example 2

[0399] Hydroxygallium naphthalocyaninetetrasulfonamide 5 was prepared according to the procedure outlined in Scheme 2.

a) hydroxygallium naphthalocyaninetetrasulfonyl chloride (ClSO2)4NcGaOH 4

[0400] Hydroxygallium naphthalocyaninetetrasulfonic acid 2 (374 mg; 0.334 mmol) from Example 1 was suspended in thionyl chloride (3 mL) containing a couple of drops of DMF. The reaction mixture was heated at 60-70° C. (bath) for 2 h under a slow stream of nitrogen, after which time the mixture became homogeneous and dark green in colour. After cooling to room temperature the resulting solution was diluted with chloroform (5 mL) and ether (50 mL) to precipitate the product. The supernatant liquid was decanted and the solid was suspended in ether (50 mL) and filtered off, washing with ether (3×10 mL). After drying under high vacuum the sulfonyl chloride 4 was obtained as a black solid (360 mg; 90%), that was insoluble in water, λmax (DMSO) 803 nm. The absorption spectrum of the sulfonyl chlorid...

example 3

[0410] Hydroxygallium naphthalocyaninetetrasulfonic acid 2, prepared in Example 1, was tested for lightfastness on Reflex Unijet 143 gsm paper, in accordance with the procedure described above. The dye was tested in formulations having dye concentrations of 2.24 mM, 4.49 mM and 7.46 mM. The reflectance spectra measured over time for each dye concentration are shown in FIGS. 33 to 35.

[0411] From these data, the following lightfastness values were estimated:

Hydroxygallium naphthalocyaninetetrasulfonic acid 2:

[0412] 2.24 mM: 39 years

[0413] 4.49 mM: 39 years

[0414] 7.46 mM 92 years

[0415] All lightfastness values were well above accepted industry standards. A significant increase in lightfastness was observed when the concentration of dye is increased to 7.46 mM.

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Abstract

There is provided an inkjet ink comprising an IR-absorbing dye of formula (I): wherein M is Ga(A1); A1 is an axial ligand selected from —OH, halogen, —OR3, —OC(O)R4, a hydrophilic ligand and / or a ligand suitable for reducing cofacial interactions; R1 and R2 may be the same or different and are selected from hydrogen or C1-12 alkoxy; R3 is selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl or Si(Rx)(Ry)(Rz); and R4 is selected from C1-12 alkyl, C5-12 aryl or C5-12 arylalkyl Rx, Ry and Rz may be the same or different and are selected from C1-12 alkyl, C5-12 aryl, C5-12 arylalkyl, C1-12 alkoxy, C5-12 aryloxy or C5-12 arylalkoxy; W is a hydrophilic group, each W group being independently selected from a substituent comprising a sulfonic acid group (including salts thereof), or a substituent comprising a sulfonamide group; n1 is 0, 1, 2 or 3; n2 is 0, 2, or 3; n3 is 0, 1, 2 or 3; n4 is 0, 1, 2 or 3; provided that at least one of n1, n2, n3 or n4 is greater than 0. Such inks are suitable for use in netpage, Hyperlabel and other applications.

Description

CROSS REFERENCE TO RELATED APPLICATIONS [0001] The present application is a continuation of U.S. application Ser. No. 10 / 986,402 Filed on Nov. 12, 2004, which is a continuation-in-part of U.S. application Ser. No. 10 / 913,381 filed on Aug. 9, 2004, the entire contents of which are herein incorporated by reference.FIELD OF THE INVENTION [0002] The present application relates to infrared (IR) dyes, in particular near-IR dyes, which are synthetically accessible in high yield and which are dispersible in an aqueous ink base. It has been developed primarily to allow facile preparation of dyes suitable for use in inkjet inks. CO-PENDING APPLICATION [0003] Various methods, systems and apparatus relating to the present invention are disclosed in the following co-pending applications filed by the applicant or assignee of the present invention: 10 / 91337510 / 91337310 / 91337410 / 91337210 / 91337710 / 91337810 / 91338010 / 91337910 / 91337610 / 986402 The disclosures of these co-pending applications are incorp...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C09D11/00G06K7/12
CPCC09B47/045C09B47/0678G06F3/03545C09D11/32C09D11/328C09B47/24C09B67/0086C09B67/009
Inventor VONWILLER, SIMONE CHARLOTTESTARLING, SCOTT MATTHEWRIDLEY, DAMON DONALDHALL, LACHLAN EVERETTFIELDER, SIMONINDUSEGARAM, SUTHARSINYSILVERBROOK, KIALAPSTUN, PAUL
Owner BASF AG
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